Effect of AI-Assisted Discharge Education on Parents of Children With Bronchitis/Bronchiolitis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorOsmaniye Korkut Ata University
About this trial
This randomized controlled trial aims to evaluate the effects of artificial intelligence-assisted discharge education on mothers of children hospitalized with bronchitis/bronchiolitis. A total of 162 mothers will be randomly assigned to one of three groups: AI-assisted written discharge education, AI-assisted video discharge education, or routine discharge education. The primary outcome will be mothers' knowledge of home care after discharge. Secondary outcomes will include anxiety, readiness for hospital discharge, and satisfaction with discharge education. The study hypothesizes that AI-assisted written and video discharge education will improve mothers' knowledge and readiness for discharge, reduce anxiety, and increase satisfaction compared with routine discharge education.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Mother of a child hospitalized with a diagnosis of bronchitis/bronchiolitis
Child hospitalized for at least 3 days
Willing to participate and provide informed consent
Able to read and understand Turkish and communicate sufficiently to complete the study forms
Disqualifiers
Unable to read/view the educational materials or complete the study forms
Child requiring intensive care, experiencing severe clinical deterioration, or having a condition preventing completion of the study
Child with an additional chronic disease or special care needs
Mother who is a healthcare professional
Trial design
Design model
Parallel
Treatments tested in this trial
AI-Assisted Written Discharge Education
BehavioralA written discharge education booklet developed with support from ChatGPT based on standard discharge content and expert review.
AI-Assisted Video Discharge Education
BehavioralA video discharge education intervention developed with support from Gemini Notebook and designed to cover the same learning objectives as the written material.
Routine Discharge Education
BehavioralStandard discharge education routinely provided by the institution.
Treatment groups
144 Participants
are divided into 3 treatment groupsGroup A: AI-Assisted Written Discharge EducationExperimental treatment 1 intervention
Group B: AI-Assisted Video Discharge EducationExperimental treatment 1 intervention
Group C: Routine Discharge EducationActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Change in Maternal Knowledge Score Regarding Home Care After Discharge
Maternal knowledge will be assessed using a 10-item true/false knowledge test developed according to the content of the discharge education. Each correct answer is scored as 1 and each incorrect answer as 0, yielding a total score ranging from 0 to 10. Higher scores indicate greater knowledge.
Time frame
Baseline before randomization and at hospital discharge, during the same hospitalization.Secondary outcomes
1
Change in Readiness for Hospital Discharge
Readiness for hospital discharge will be assessed using the 26-item Pediatric Readiness for Hospital Discharge Scale (Ped-RHDS). Higher scores indicate greater readiness for hospital discharge.
Time frame
Baseline before randomization and at hospital discharge, during the same hospitalization2
Change in Maternal Anxiety Level
Maternal anxiety will be assessed using a Visual Analog Scale (VAS) ranging from 0 to 10, where 0 indicates no anxiety and 10 indicates the highest level of anxiety. Higher scores indicate greater anxiety.
Time frame
Baseline before randomization and at hospital discharge, during the same hospitalization.3
Maternal Satisfaction With Discharge Education
Satisfaction with discharge education will be assessed using a Visual Analog Scale (VAS) ranging from 0 to 10, with higher scores indicating greater satisfaction with the discharge education.
Time frame
At hospital discharge, during the same hospitalization.Sponsors and contacts
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Source ClinicalTrials.gov
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